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Ortho Band L/C 5gm

FDA UDI

Class II (US FDA UDI)

by Bisco Inc.

Identity

Trade Name
Ortho Band L/C 5gm FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Model / Reference
F-6411 FDA UDI

Identifiers

Catalog Number
F-6411 FDA UDI
Primary DI / UDI-DI
D757F64110 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dentine bonding agent/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Ortho Band L/C 5gm by Bisco Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bisco Inc.

Sources (1)

  • FDA UDI d5a67b65-c837-4b07-9370-7f7685586aa6 37 fields · synced May 31, 2026